Euromed Communications
Euromed Communications was established over 10 years ago and has a core of qualified professionals supplemented by a team of expert medical and scientific researchers, producing publications for the scientific community, inexpensively, accurately and rapidly.
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FDA Requirements - extending sales to the United States
Reprinted from the Medical Devices Manual Maria Donawa provides an overview of the United States Food and Drug Administration (FDA) requirements for medical devices, including in vitro diagnostic medical devices.
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Environmental regulation and compliance for medical devices
Reprinted from the Medical Devices Manual George Howarth discusses the environmental legislation that has been introduced directed at minimising the environmental damage associated with products which includes medical devices.
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Canadian regulations for medical devices
Reprinted from the Medical Devices Manual Bernard Tremaine addresses the main regulatory issues concerning the placing of or making available for sale, medical devices on the Canadian market.
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MedDRA : Medical Dictionary for Regulatory Activities
Reprinted from the Clinical Research Manual, Christina Winter provides general information on the development and structure of the dictionary, and provides the latest information on how to implement and use MedDRA.
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Simulation of clinical trials
Reprinted from the Clinical Research Manual, Tony Greenfield describes and illustrates discrete event simulation, as applied to phase three studies, which can help prevent costly mistakes and monitors likely completion times and outcomes.
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